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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0100001"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://www.ebi.ac.uk/efo/EFO_1000159 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_1000159">
        <rdfs:label>obsolete_Cerebellar Liponeurocytoma</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.w3.org/2002/07/owl#Thing"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/10642/cerebellar-liponeurocytoma</rdfs:seeAlso>
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        <oboInOwl:hasExactSynonym>cerebellar liponeurocytoma (WHO grade II)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:716592003</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:1000159</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C6905</oboInOwl:hasDbXref>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0006131</ns4:IAO_0100001>
        <oboInOwl:hasExactSynonym>lipomatous medulloblastoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:6458</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010642</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:251931</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>cerebellar liponeurocytoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1370507</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ONCOTREE:CLNC</oboInOwl:hasDbXref>
        <ns5:reason_for_obsolescence>Replaced by Mondo term MONDO_0006131, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0006131</ns5:reason_for_obsolescence>
        <ns5:obsoleted_in_version>3.88.0</ns5:obsoleted_in_version>
        <oboInOwl:hasRelatedSynonym>CLNC</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>lipomatous medulloblastoma (formerly)</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>A rare, WHO grade II cerebellar neoplasm which shows consistent neuronal, variable astrocytic and focal lipomatous differentiation. It occurs in adults, has a low proliferative potential and usually has a favorable prognosis. (Adapted from WHO)</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>ICDO:0000/0</oboInOwl:hasDbXref>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disease"/>
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